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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230744Generated: October 30, 2026

Diisopropylethylamine → tert-Butyl 1-(4-(3-(4-fluorophenylamino)-3-oxopropanamido)phenyl)-1H-pyrrolo[3,2-c]pyridin-4-ylcarbamate

https://huagongshe.com/reaction/230744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant3-(4-Fluorophenylamino)-3-oxopropanoic acidHCID 4341843—
ReactantTert-butyl 1-(4-aminophenyl)-1h-pyrrolo[3,2-c]pyridin-4-ylcarbamateHCID 57763144—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 1-(4-(3-(4-fluorophenylamino)-3-oxopropanamido)phenyl)-1H-pyrrolo[3,2-c]pyridin-4-ylcarbamateHCID 5776315156,524,596%

Reaction Steps

A solution of tert-butyl 1-(4-aminophenyl)-1H-pyrrolo[3,2-c]pyridin-4-ylcarbamate (27 mg, 0.083 mmol, Compound B of Example 1) in DMF (1 mL) was treated with 3-(4-fluorophenylamino)-3-oxopropanoic acid (25 mg, 0.13 nmol), DIPEA (21 μL, 0.13 mmol) and TBTU (40 mg, 0.13 mmol) and the mixture stirred at RT for 16 h. The mixture was concentrated in vacuo to remove the DMF and the residue was partitioned between EtOAc (2 mL) and saturated sodium bicarbonate solution (2 mL). The EtOAc phase was washed with 10% aqueous LiCl (2 mL), brine (2 mL), dried (MgSO4) and concentrated in vacuo. The crude product was purified using a Chromatotron (1 mm SiO2 GF rotor, 2-5% MeOH-CHCl3 gradient elution) to give the title compound (37 mg, 88%) as an off-white solid. LCMS (ESI+) m/z 504 (M+H)+; HPLC tR=3.49 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566784B2
Source datasetuspto-grants-2009_07
ORD IDord-afb498b2ff5a4ae1b44417f73cea8223
Source noteuspto-grants-2009_07